Trifluoroacetic acid → HCID 59279572, compound
Reaction equation
C(C(O)=O)(F)(F)F.[O:8]=[C:9]1[N:13]([CH2:14][C:15]([O:17]C(C)(C)C)=[O:16])[C:12]2[CH:22]=[CH:23][CH:24]=[CH:25][C:11]=2[N:10]1[CH:26]1[CH2:31][CH2:30][S:29][CH2:28][CH2:27]1>C(Cl)Cl>[O:8]=[C:9]1[N:13]([CH2:14][C:15]([OH:17])=[O:16])[C:12]2[CH:22]=[CH:23][CH:24]=[CH:25][C:11]=2[N:10]1[CH:26]1[CH2:31][CH2:30][S:29][CH2:28][CH2:27]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
CF3CO2H (1 mL) was added to a solution of tert-butyl (2-oxo-3-tetrahydro-2H-thiopyran-4-yl-2,3-dihydro-1H-benzimidazol-1-yl)acetate from Step C (169 mg, 0.485 mmol) in CH2Cl2 (3 mL). After 3 h, the mixture was concentrated in vacuo to give the title compound. MS: m/z=293 (M+1).
Workup
- concentrationthe mixture was concentrated in vacuo
Sources & evidence
- ORD record
- ord-00d1c81ca98140f9b06256f0561e18f3
- Source dataset
- uspto-grants-2011_08
- Patent number
- US08003792B2
Reaction notes
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